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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2261796Generated: November 3, 2026

4-Iodo-3-methylbenzoic acid → (4-Iodo-3-methylphenyl)methanol

https://huagongshe.com/reaction/2261796

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Iodo-3-methylbenzoic acidHCID 1517322—
SolventTetrahydrofuranHCID 8028—
Product(4-Iodo-3-methylphenyl)methanolHCID 5384360195%

Reaction Steps

To a solution of 4-Iodo-3-methyl-benzoic acid (5.2 g, 20 mmol) in THF (30 mL) is added 2.0 M borane-dimethyl sulfide complex in THF (40.0 mL, 80 mmol) dropwise. The mixture is stirred overnight. The reaction mixture is quenched carefully at 0° C. with methanol (20 mL) and the mixture is evaporated to dryness under reduced pressure. The residue is partitioned between EtOAc (80 mL) and water (60 mL). The organic phase is washed with brine (60 mL), dried (Na2SO4), filtered, and concentrated under reduced pressure to a residue. The residue is purified by flash chromatography (gradient EtOAc/Hexane) to afford the title compound as white solid (4.7 g, 95%). 1HNMR (CDCl3) (ppm): 2.4 (3H, s), 4.55 (2H, s), 6.8-7.75 (3H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07846960B2
Source datasetuspto-grants-2010_12
ORD IDord-713ab97a6e7d44c9901643bfca98c9e4
Source noteuspto-grants-2010_12